𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population

✍ Scribed by Jara, Lilian; Aspillaga, Manuel; Avenda�o, Isabel; Obreque, Victor; Blanco, Rafael; Valenzuela, Carlos Y.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
39 KB
Volume
75
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19980123)75:3<277::aid-ajmg10>3.0.co;2-m

No coin nor oath required. For personal study only.

✦ Synopsis


We report on the allele distribution in a normal Chilean population at 2 microsatellite loci neighbouring the FRAXA locus and at the CGG repeat in the 5 end of the FMR-1 gene, which causes the fragile X syndrome. The most common CGG repeat allele was 30 (41.7%), with 29 being second most common (30.2%). This distribution was similar from that seen in Caucasians but different from that observed in Chinese controls, where the most common allele was 29 repeats. Four alleles of FRAXAC1 and 6 of DXS548 were observed in the Chilean sample. A striking linkage disequilibrium of FMR-1 alleles with FRAXAC1 alleles was observed. In 90% of the 30 CGG repeat alleles only 31% of the 29 CGG repeat alleles had the FRAXAC1 154 bp allele. This result is in agreement with the suggestion that slippage between CGG repeat alleles 29 and 30 and between 152 and 154 FRAXAC1 alleles is very rare. This study suggests a founder chromosome effect in the Chilean population. Am.


📜 SIMILAR VOLUMES


Mosaicism for full mutation and normal-s
✍ Orrico, Alfredo; Galli, Lucia; Dotti, Maria Teresa; Plewnia, Katrin; Censini, St 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 15 KB 👁 2 views

The main mutation in fragile X patients is the expansion of the CGG repeat in the first exon of the FMR1 gene, associated with hypermethylation of the proximal CpG island. An increasing number of atypical cases have been reported showing the coexistence of full mutation and premutated or normalsized

CAG repeat sequences in bipolar affectiv
✍ Zander, Cecilia; Sch�rhoff, Franck; Laurent, Claudine; Chavand, Olivier; Bellivi 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 19 KB 👁 1 views

Anticipation has been described in bipolar affective disorder (BPAD). However, there are conflicting results from association studies screening for a link between BPAD and CAG/CTG repeat expansions, the molecular basis of anticipation in several hereditary neurodegenerative disorders. Here, the repe

Instability of the FMR2 trinucleotide re
✍ Brown, T. C.; Tarleton, J. C.; Go, R. C. P.; Longshore, J. W.; Descartes, M. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 62 KB 👁 1 views

The fragile sites FRAXA and FRAXE, located ∼600 kb apart on Xq27.3 and Xq28, respectively, are due to a CGG trinucleotide repeat expansion. Although the expansion mechanism for these and other trinucleotide repeat disorders remains unknown, the similarities between the FRAXA and FRAXE regions sugges

cover
✍ David W Robinson 📂 Fiction 📅 2014 🏛 Crooked Cat Books 🌐 English ⚖ 150 KB 👁 2 views
Genetic variation and intergenerationalF
✍ Patsalis, P.C.; Sismani, C.; Stylianou, S.; Ioannou, P.; Joseph, G.; Manoli, P.; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 20 KB

In order to identify genetic factors governing expansion of the CGG repeat in the FMR1 gene and to determine what predisposes or causes a normal stable allele to change to an unstable premutation allele, it is essential to study and understand the basis of normal variation. The aim of this study was

Two new polymorphisms in the arylsulfata
✍ Coulter-Mackie, Marion; Gagnier, Liane 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 21 KB 👁 1 views

Linkage disequilibrium exists between metachromatic leukodystrophy (MLD) and pseudodeficiency mutations and selected polymorphisms within the arylsulfatase A gene. We have identified 2 new polymorphic NlaIII sites, NlaIII 1 and NlaIII 2 , in the gene that, when used in combination with the known Bsr